BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    DIRECT ELISA FOR HERPES SIMPLEX VIRUS

    K Number: K853307 · Decision Dec 23, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    33
    Applicant Total
    7
    Review Days
    138

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    Basic Information

    Device Name
    DIRECT ELISA FOR HERPES SIMPLEX VIRUS
    K Number
    K853307
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3305
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Fairleigh Dickinson Laboratories, Inc.
    Date Received
    August 7, 1985
    Decision Date
    December 23, 1985
    Product Code
    GQN
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GQN Antigen, Cf (Including Cf Control), Herpesvirus Hominis 1,2

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